NDC 62756-520 – Sumatriptan succinate

Sumatriptan Succinate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC62756-520

Product details

Brand name
Sumatriptan succinate
Generic name
Sumatriptan succinate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078295
Marketed since
August 10, 2009
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Sumatriptan Succinate →

Package NDC codes (5)

Package NDCDescriptionSince
62756-520-013 BLISTER PACK in 1 CARTON (62756-520-01) / 9 TABLET, FILM COATED in 1 BLISTER PACKNov 1, 2020
62756-520-08100 TABLET, FILM COATED in 1 BOTTLE (62756-520-08)Aug 10, 2009
62756-520-181000 TABLET, FILM COATED in 1 BOTTLE (62756-520-18)Aug 10, 2009
62756-520-8330 TABLET, FILM COATED in 1 BOTTLE (62756-520-83)Aug 10, 2009
62756-520-939 BLISTER PACK in 1 CARTON (62756-520-93) / 1 TABLET, FILM COATED in 1 BLISTER PACKAug 10, 2009

Recalls mentioning this NDC

Other Sumatriptan Succinate products